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While tissue engineering may allow formation of custom implants.
Ero1 α induction by PAC-1 may allow formation of microdomains of calcium channels, leading to selective uptake of calcium into mitochondria through mitochondrial Ca2+ uniporter (MUC).
This transient coordination site may allow formation of a μ-1,2-peroxo-diferric species, which is the most commonly proposed precursor to high-valent iron oxo species in non-heme diiron-carboxylate enzymes.
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Conservation of these stem cells when treating immature teeth may allow continuous formation of the root to completion.
A longer duration may allow the formation of epileptogenic foci, leading to chronic epilepsy, and eventually have a negative effect on the prognosis of the patients.
Indeed, this process may allow the formation of new genes from pre-existing ones.
In societies that are polarized, or fragmented by multiple cleavages, a multiparty system with proportional representation may allow the formation of alternative coalitions (as in Belgium, for example), and thus forestall dangerous zero-sum outcomes.
Similarly, a narrow window early in the ontogeny of colonial marine invertebrates, prior to the development of the allorecognition system, may allow the formation of chimeric entities [53].
The lack of the terminal proline residue in mammalian STIM2 may allow the formation of a short amphipathic α-helix.
Smaller side chains in this region may allow the formation of the aberrant (7 R -homobisabolyl cation inteR -homobisabolylerved for F198L EIZS.
Ero1 α upregulation may allow the formation of mitochondria-associated ER membrane (MAM), leading to mitochondrial calcium uptake resulting in mitochondrial permeabilization.
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